Browse by Current Cardiff authors

Rammos, Alexandros, Blakey, Rachel, Dennison, Charlotte ORCID: https://orcid.org/0000-0002-7493-2041, Lewis, Sarah, Ali, Nabila, Davies, Amy, Wren, Yvonne, Humphries, Kerry, Sandy, Jonathan, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Kendall, Kimberley ORCID: https://orcid.org/0000-0002-6755-6121, Sharp, Gemma, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 and Stergiakouli, Evie 2025. Copy number variants and their implications for developmental and behavioural problems in cleft lip and/or palate. Human Molecular Genetics Item availability restricted.

Tume, Claire E., Chick, Sophie L., Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Cameron, Darren and Bray, Nicholas J. ORCID: https://orcid.org/0000-0002-4357-574X 2024. Genetic implication of specific glutamatergic neurons of the prefrontal cortex in the pathophysiology of schizophrenia. Biological Psychiatry 4 (5) , 100345. 10.1016/j.bpsgos.2024.100345

Legge, Sophie E., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Woolway, Grace, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Cardno, Alastair G., Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael J. ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2024. Genetic and phenotypic features of Schizophrenia in the UK Biobank. JAMA Psychiatry 81 , pp. 681-690. 10.1001/jamapsychiatry.2024.0200

Kappel, Djenifer, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Fenner, Eilidh, King, Adrian, Jansen, John, Helthius, Marinka, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 and Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590 2024. Rare variants in pharmacogenes influence clozapine metabolism in individuals with schizophrenia. European Neuropsychopharmacology 80 , pp. 47-54. 10.1016/j.euroneuro.2023.12.007

Wellard, Natalie L., Clifton, Nicholas E. ORCID: https://orcid.org/0000-0003-2597-5253, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Thomas, Kerrie L. ORCID: https://orcid.org/0000-0003-3355-9583 and Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 2024. The association of hippocampal long-term potentiation-induced gene expression with genetic risk for psychosis. International Journal of Molecular Sciences 25 (2) , 946. 10.3390/ijms25020946

Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Legge, Sophie, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2023. Genomic findings in schizophrenia and their implications. Molecular Psychiatry 28 , pp. 3638-3647. 10.1038/s41380-023-02293-8

Rammos, Alexandros, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Hubbard, Leon, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222 2023. Family-based analysis of the contribution of rare and common genetic variants to school performance in schizophrenia. Molecular Psychiatry 28 , pp. 2081-2087. 10.1038/s41380-023-02013-2

Wadon, Megan, Fenner, Eilidh, Kendall, Kimberley ORCID: https://orcid.org/0000-0002-6755-6121, Bailey, Grace, Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222 and Peall, Kathryn J. ORCID: https://orcid.org/0000-0003-4749-4944 2022. Clinical and genotypic analysis in determining dystonia non-motor phenotypic heterogeneity: a UK Biobank study. Journal of Neurology 269 , pp. 6436-6451. 10.1007/s00415-022-11307-4

Clifton, Nicholas ORCID: https://orcid.org/0000-0003-2597-5253, Bosworth, Matthew ORCID: https://orcid.org/0000-0003-1391-7515, Haan, Niels, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Wilkinson, Lawrence ORCID: https://orcid.org/0000-0002-9337-6124, Isles, Anthony ORCID: https://orcid.org/0000-0002-7587-5712, Collins, Mark and Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 2022. Developmental disruption to the cortical transcriptome and synaptosome in a model of SETD1A loss-of-function. Human Molecular Genetics 31 (18) , pp. 3095-3106. 10.1093/hmg/ddac105

Bracher-Smith, Matthew, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Menzies, Georgina ORCID: https://orcid.org/0000-0002-6600-6507, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 2022. Machine learning for prediction of schizophrenia using genetic and demographic factors in the UK Biobank. Schizophrenia Research 246 , pp. 156-164. 10.1016/j.schres.2022.06.006

Creeth, Hugo D. J., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Legge, Sophie E., Dennison, Charlotte A. ORCID: https://orcid.org/0000-0002-7493-2041, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2022. Ultrarare coding variants and cognitive function in schizophrenia. JAMA Psychiatry 79 (10) , pp. 963-970. 10.1001/jamapsychiatry.2022.2289

McAllister, Branduff, Donaldson, Jasmine ORCID: https://orcid.org/0000-0001-6699-0674, Binda, Caroline, Powell, Sophie, Chughtai, Uroosa, Edwards, Gareth, Stone, Joseph, Lobanov, Sergey ORCID: https://orcid.org/0000-0002-3126-1903, Elliston, Linda, Schuhmacher, Laura, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Menzies, Georgina ORCID: https://orcid.org/0000-0002-6600-6507, Ciosi, Marc, Maxwell, Alastair, Chao, Michael, Eun Pyo, Hong, Lucente, Diane, Wheeler, Vanessa, Jong-Min, Lee, MacDonald, Marcy, Long, Jeffrey, Aylward, Elizabeth, Landwehrmeyer, G. Bernhard, Rosser, Anne ORCID: https://orcid.org/0000-0002-4716-4753, REGISTRY Investigators of the European Huntington’s disease netw, Paulsen, Jane, PREDICT-HD Investigators of the Huntington Study Group, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Gusella, James, Monckton, Darren, Allen, Nicholas, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612 and Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131 2022. Exome sequencing of individuals with Huntington’s disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset. Nature Neuroscience 25 , pp. 446-457. 10.1038/s41593-022-01033-5

Singh, Tarjinder, Schizophrenia Exome Meta-Analysis (SCHEMA) Consortium, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2022. Rare coding variants in ten genes confer substantial risk for schizophrenia. Nature 604 , pp. 509-516. 10.1038/s41586-022-04556-w

Sanders, Bret, D'Andrea, Daniel, Collins, Mark O., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Steward, Tom G. J., Zhu, Ying, Chapman, Gareth, Legge, Sophie E., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Harwood, Adrian J. ORCID: https://orcid.org/0000-0003-3124-5169, Gray, William P. ORCID: https://orcid.org/0000-0001-7595-8887, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Errington, Adam C. ORCID: https://orcid.org/0000-0002-2171-389X, Blake, Derek J. ORCID: https://orcid.org/0000-0002-5005-4731, Whitcomb, Daniel J., Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452 and Shin, Eunju ORCID: https://orcid.org/0000-0002-8865-6834 2022. Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants. Nature Communications 13 (1) , 27. 10.1038/s41467-021-27601-0

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Creeth, Hugo, Hwo, Hai-Gwo, Chen, Wei J., Tsuang, Ming, Glatt, Stephen J., Rey, Romain, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2021. Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations. Nature Communications 12 , 5353. 10.1038/s41467-021-25532-4

Legge, Sophie, Cardno, Alastair, Allardyce, Judith ORCID: https://orcid.org/0000-0003-4094-552X, Dennison, Charlotte ORCID: https://orcid.org/0000-0002-7493-2041, Hubbard, Leon, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Richards, Alexander, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2021. Associations between schizophrenia polygenic liability, symptom dimensions, and cognitive ability in schizophrenia. JAMA Psychiatry 78 (10) , pp. 1143-1151. 10.1001/jamapsychiatry.2021.1961

Clifton, Nicholas E. ORCID: https://orcid.org/0000-0003-2597-5253, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412, Pardinas, Antonio. F. ORCID: https://orcid.org/0000-0001-6845-7590, Harwood, Janet, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, O’Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 and Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452 2021. Genetic association of FMRP targets with psychiatric disorders. Molecular Psychiatry 26 , pp. 2977-2990. 10.1038/s41380-020-00912-2

Hubbard, Leon, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Morris, Derek W., Lynham, Amy J. ORCID: https://orcid.org/0000-0002-3189-6888, Richards, Alex L., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Legge, Sophie E., Harold, Denise, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Corvin, Aiden C., Gill, Michael G., Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Donohoe, Gary, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452 and Walters, James T.R. ORCID: https://orcid.org/0000-0002-6980-4053 2021. Rare copy number variations are associated with poorer cognition in schizophrenia. Biological Psychiatry 90 (1) , pp. 28-34. 10.1016/j.biopsych.2020.11.025

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2021. Copy number variation and neuropsychiatric illness. Current Opinion in Genetics and Development 68 , pp. 57-63. 10.1016/j.gde.2021.02.014

Caseras, Xavier ORCID: https://orcid.org/0000-0002-8490-6891, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Legge, Sophie E., Bracher-Smith, Matthew, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 and Murphy, Kevin ORCID: https://orcid.org/0000-0002-6516-313X 2021. Effects of genomic copy number variants penetrant for schizophrenia on cortical thickness and surface area in healthy individuals: analysis of the UK Biobank. British Journal of Psychiatry 218 (2) , pp. 104-111. 10.1192/bjp.2020.139

Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, John, Ann, Lee, Sze Chim, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Pardiñas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Del Pozo Banos, Marcos, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O’Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Lloyd, Keith, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Legge, Sophie E. and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2020. Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: a data linkage study. BJPsych Open 6 (6) , e139. 10.1192/bjo.2020.42

Legge, Sophie, Dennison, Charlotte ORCID: https://orcid.org/0000-0002-7493-2041, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Hopkins, Lucinda, Bates, Lesley, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 2020. Clinical indicators of treatment-resistant psychosis. British Journal of Psychiatry 216 (5) , pp. 259-266. 10.1192/bjp.2019.120

Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Hosking, Grace, Wadon, Megan, Agha, Sharifah Shameem ORCID: https://orcid.org/0000-0001-9541-6786, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2020. A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder. Translational Psychiatry 10 , 135. 10.1038/s41398-020-0821-y

Warland, Anthony, Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Caseras, Xavier ORCID: https://orcid.org/0000-0002-8490-6891 2020. Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank. Molecular Psychiatry 25 (4) , pp. 854-862. 10.1038/s41380-019-0355-y

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222 and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2020. Translating insights from neuropsychiatric genetics and genomics for precision psychiatry. Genome Medicine 12 (1) , 43. 10.1186/s13073-020-00734-5

Szatkiewicz, Jin P., Fromer, Menachem, Nonneman, Randal J., Ancalade, NaEshia, Johnson, Jessica S., Stahl, Eli A., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Bergen, Sarah, Hultman, Christina, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Sklar, Pamela, Sullivan, Patrick F., Purcell, Shaun M., Crowley, James J. and Ruderfer, Douglas M. 2020. Characterization of single gene copy number variants in schizophrenia. Biological Psychiatry 87 (8) , pp. 736-744. 10.1016/j.biopsych.2019.09.023

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, GROUP Investigators, Han, Jun, Morgan, Joanne, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452, Duffield, Madeleine, Hall, Lynsey S., Legge, Sophie E., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Richards, Alexander L., Roth, Julian, Lezheiko, Tatyana, Kondratyev, Nikolay, Golimbat, Vera, Parellada, Mara, González-Peñas, Javier, Arango, Celso, Gawlik, Micha, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2020. De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia. Nature Neuroscience 23 (2) , pp. 179-184. 10.1038/s41593-019-0565-2

Hall, Lynsey S, Medway, Christopher W ORCID: https://orcid.org/0000-0002-1764-0587, Pain, Oliver, Pardinas, Antonio F ORCID: https://orcid.org/0000-0001-6845-7590, Rees, Elliott G ORCID: https://orcid.org/0000-0002-6168-9222, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Bray, Nicholas J ORCID: https://orcid.org/0000-0002-4357-574X, Holmans, Peter A ORCID: https://orcid.org/0000-0003-0870-9412, Walters, James T R ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2020. A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia. Human Molecular Genetics 29 (1) , pp. 159-167. 10.1093/hmg/ddz253

Legge, Sophie E., Jones, Hannah J., Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Menzies, Georgina ORCID: https://orcid.org/0000-0002-6600-6507, Bracher-Smith, Matthew, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Davis, Katrina A., Hotopf, Matthew, Savage, Jeanne E., Posthuma, Danielle, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211 and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2019. Association of genetic liability to psychotic experiences with neuropsychotic disorders and traits. JAMA Psychiatry 76 (12) , pp. 1256-1265. 10.1001/jamapsychiatry.2019.2508

Chapman, Ria M, Tinsley, Caroline L, Hill, Matthew J ORCID: https://orcid.org/0000-0001-6776-8709, Forrest, Marc P, Tansey, Katherine E, Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Doyle, A. Michelle, Wilkinson, Lawrence S. ORCID: https://orcid.org/0000-0002-9337-6124, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Blake, Derek J. ORCID: https://orcid.org/0000-0002-5005-4731 2019. Convergent evidence that ZNF804A is a regulator of pre-messenger RNA processing and gene expression. Schizophrenia Bulletin 45 (6) , pp. 1267-1278. 10.1093/schbul/sby183

Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, Bracher-Smith, Matthew, Fitzpatrick, Harry, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James T.R. ORCID: https://orcid.org/0000-0002-6980-4053 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2019. Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank. British Journal of Psychiatry 214 (05) , pp. 297-304. 10.1192/bjp.2018.301

Kendall, Kimberley M ORCID: https://orcid.org/0000-0002-6755-6121, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Bracher-Smith, Matthew, Legge, Sophie, Riglin, Lucy, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053 2019. Association of rare copy number variants with risk of depression. JAMA Psychiatry 76 (8) , pp. 818-825. 10.1001/jamapsychiatry.2019.0566

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Morgan, Joanne, Hambridge, Kirsty, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452, Richards, Alexander L., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, McDonald, Colm, Donohoe, Gary, Morris, Derek W., Kenny, Elaine, Kelleher, Eric, Gill, Michael, Corvin, Aiden, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 2019. Targeted sequencing of 10,198 samples confirms abnormalities in neuronal activity and implicates voltage-gated sodium channels in schizophrenia pathogenesis. Biological Psychiatry 85 (7) , pp. 554-562. 10.1016/j.biopsych.2018.08.022

Vadgama, Nirmal, Pittman, Alan, Simpson, Michael, Nirmalananthan, Niranjanan, Murray, Robin, Yoshikawa, Takeo, De Rijk, Peter, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Hughes, Deborah, Fitzgerald, Tomas, Kristiansen, Mark, Pearce, Kerra, Cerveira, Eliza, Zhu, Qihui, Zhang, Chengsheng, Lee, Charles, Hardy, John and Nasir, Jamal 2019. De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes. European Journal of Human Genetics 27 (7) , pp. 1121-1133. 10.1038/s41431-019-0376-7

Drakesmith, Mark ORCID: https://orcid.org/0000-0001-8574-9560, Parker, Greg D., Smith, Jacqueline, Linden, Stefanie C., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Jones, Derek K. ORCID: https://orcid.org/0000-0003-4409-8049 and Linden, David E. J. 2019. Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white-matter structures. Translational Psychiatry 9 (1) , 102. 10.1038/s41398-019-0440-7

Crawford, Karen, Bracher-Smith, Matthew, Owen, David ORCID: https://orcid.org/0000-0003-4798-0862, Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Pardinas, Antonio F., Einon, Mark ORCID: https://orcid.org/0000-0003-3797-7352, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2019. Medical consequences of pathogenic CNVs in adults: Analysis of the UK Biobank. Journal of Medical Genetics 56 , pp. 131-138. 10.1136/jmedgenet-2018-105477

Owen, David ORCID: https://orcid.org/0000-0003-4798-0862, Bracher Smith, Mathew, Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Einon, Mark ORCID: https://orcid.org/0000-0003-3797-7352, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2018. Effects of pathogenic CNVs on physical traits in participants of the UK Biobank. BMC Genomics 19 (1) , 867. 10.1186/s12864-018-5292-7

Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, GERAD Consortium, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Ripke, Stephan, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L. ORCID: https://orcid.org/0000-0002-8990-0958, Han, Jun, Hubbard, Leon, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Mantripragada, Kiran ORCID: https://orcid.org/0000-0003-2070-8105, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, MacCabe, James H., McCarroll, Steven A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda, Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nichols G., McIntosh, Andrew M., Plomin, Robert P., Porteous, David J., Wray, Naomi R., Caballero, Armando, Geschwind, Daniel H., Huckins, Laura M., Ruderfer, Douglas M., Santiago, Enrique, Sklar, Pamela, Stahl, Eli A., Won, Hyejung, Agerbo, Eeben A., Als, Thomas P., Andreassen, Ole A., Bækvad-Hansen, Marie, Mortensen, Preben Bo, Pedersen, Carsten Bocker, Børglum, Anders D., Bybjerg-Grauholm, Jonas, Djurovic, Srdjan, Durmishi, Naser, Giørtz Pedersenu, Marianne, Golimbet, Vera, Grove, Jakob, Hougaard, David M., Mattheisen, Manuel, Molden, Espen, Mors, Ole, Nordentoft, Merete, Pejovic-Milovancevic, Milica, Sigurdsson, Engilbert, Silagadze, Teimuraz, Søholm Hansen, Christine, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Tosato, Sarah, Werge, Thomas, Collier, David A., Rujescu, Dan, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael J ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and CRESTAR Consortium 2018. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics 50 , pp. 381-389. 10.1038/s41588-018-0059-2

Legge, S. E., Hamshere, M. L. ORCID: https://orcid.org/0000-0002-8990-0958, Ripke, S., Pardinas, A. F. ORCID: https://orcid.org/0000-0001-6845-7590, Goldstein, J. I., Rees, E. ORCID: https://orcid.org/0000-0002-6168-9222, Richards, A. L., Leonenko, G. ORCID: https://orcid.org/0000-0001-8025-661X, Jorskog, L. F., Goldstein, J. I., Jarskog, L. F., Hilliard, C., Alfirevic, A., Duncan, L., Fourches, D., Huang, H., Lek, M., Neale, B. M., Ripke, S., Shianna, K., Szatkiewicz, J. P., Tropsha, A., van den Oord, E. J. C. G., Cascorbi, I., Dettling, M., Gazit, E., Goff, D. C., Holden, A. L., Kelly, D. L., Malhotra, A. K, Nielsen, J., Pirmohamed, M., Rujescu, D., Werge, T., Levy, D. L., Josiassen, R. C., Kennedy, J. L., Lieberman, J. A., Daly, M. J., Sullivan, P. F., Chambert, K. D., Collier, D. A., Genovese, G., Giegling, I., Holmans, P. ORCID: https://orcid.org/0000-0003-0870-9412, Jonasdottir, A., Kirov, G. ORCID: https://orcid.org/0000-0002-3427-3950, McCarroll, S. A., MacCabe, J. H., Mantripragada, K ORCID: https://orcid.org/0000-0003-2070-8105, Moran, J. L., Neale, B. M., Stefansson, H., Rujescu, D., Daly, M. J., Sullivan, P. F., Owen, M. J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, M. C. ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, J.T. R ORCID: https://orcid.org/0000-0002-6980-4053 2017. Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia. Molecular Psychiatry 22 , pp. 1502-1508. 10.1038/mp.2016.97

Singh, Tarjinder, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Johnstone, Mandy, Curtis, David, Suvisaari, Jaana, Torniainen, Minna, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Iyegbe, Conrad, Blackwood, Douglas, McIntosh, Andrew M., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Geschwind, Daniel, Murray, Robin M, Di Forti, Marta, Bramon, Elvira, Gandal, Michael, Hultman, Christina M., Sklar, Pamela, Palotie, Aarno, Sullivan, Patrick F., O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Barrett, Jeffrey C. 2017. The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability. Nature Genetics 49 , pp. 1167-1173. 10.1038/ng.3903

Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Einon, Mark ORCID: https://orcid.org/0000-0003-3797-7352, Thomas, Rhys ORCID: https://orcid.org/0000-0003-2062-8623, Hewitt, Jonathan ORCID: https://orcid.org/0000-0002-7924-1792, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2017. Cognitive performance among carriers of pathogenic copy number variants: analysis of 152,000 UK Biobank subjects. Biological Psychiatry 82 (2) , P103-110. 10.1016/j.biopsych.2016.08.014

Huang, Alden Y., Yu, Dongmei, Davis, Lea K., Sul, Jae Hoon, Tsetsos, Fotis, Ramensky, Vasily, Zelaya, Ivette, Ramos, Eliana Marisa, Osiecki, Lisa, Chen, Jason A., McGrath, Lauren M., Illmann, Cornelia, Sandor, Paul, Barr, Cathy L., Grados, Marco, Singer, Harvey S., Nöthen, Markus M., Hebebrand, Johannes, King, Robert A., Dion, Yves, Rouleau, Guy, Budman, Cathy L., Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Müller-Vahl, Kirsten R., Stuhrmann, Manfred, Aschauer, Harald, Stamenkovic, Mara, Schloegelhofer, Monika, Konstantinidis, Anastasios, Lyon, Gholson J., McMahon, William M., Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Batterson, James R., Rizzo, Renata, Cath, Danielle C., Wolanczyk, Tomasz, Berlin, Cheston, Malaty, Irene A., Okun, Michael S., Woods, Douglas W., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Pato, Carlos N., Pato, Michele T., Knowles, James A., Posthuma, Danielle, Pauls, David L., Cox, Nancy J., Neale, Benjamin M., Freimer, Nelson B., Paschou, Peristera, Mathews, Carol A., Scharf, Jeremiah M. and Coppola, Giovanni 2017. Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette Syndrome. Neuron 94 (6) , 1101-1111.e7. 10.1016/j.neuron.2017.06.010

Clifton, N. E. ORCID: https://orcid.org/0000-0003-2597-5253, Pocklington, A. J. ORCID: https://orcid.org/0000-0002-2137-0452, Scholz, B., Rees, E. ORCID: https://orcid.org/0000-0002-6168-9222, Walters, J. T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Kirov, G. ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, M. C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, M. J. ORCID: https://orcid.org/0000-0003-4798-0862, Wilkinson, L. S. ORCID: https://orcid.org/0000-0002-9337-6124, Thomas, K. L. ORCID: https://orcid.org/0000-0003-3355-9583 and Hall, J. ORCID: https://orcid.org/0000-0003-2737-9009 2017. Schizophrenia copy number variants and associative learning. Molecular Psychiatry 22 (2) , pp. 178-182. 10.1038/mp.2016.227

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Kendall, Kimberley ORCID: https://orcid.org/0000-0002-6755-6121, Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Legge, Sophie E., Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, MacCabe, James H., Collier, David A., Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2016. Analysis of intellectual disability copy number variants for association with schizophrenia. JAMA Psychiatry 73 (9) , pp. 963-969. 10.1001/jamapsychiatry.2016.1831

Tansey, K. E., Rees, E. ORCID: https://orcid.org/0000-0002-6168-9222, Linden, D. E. ORCID: https://orcid.org/0000-0002-5638-9292, Ripke, S., Chambert, D., Moran, J. L., McCarroll, S. A., Holmans, P. ORCID: https://orcid.org/0000-0003-0870-9412, Kirov, G. ORCID: https://orcid.org/0000-0002-3427-3950, Walters, J. ORCID: https://orcid.org/0000-0002-6980-4053, Owen, M. J. ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, M. C. ORCID: https://orcid.org/0000-0001-7073-2379 2016. Common alleles contribute to schizophrenia in CNV carriers. Molecular Psychiatry 21 , pp. 1085-1089. 10.1038/mp.2015.143

Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Ripke, Stephan, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L. ORCID: https://orcid.org/0000-0002-8990-0958, Han, Jun, Hubbard, Leon, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Mantripragada, Kiran ORCID: https://orcid.org/0000-0003-2070-8105, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, MacCabe, James H., McCarroll, Stephen A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M., Plomin, Robert, Porteous, David J., Wray, Naomi R., Consortium, Collier, David A., Rujescu, Dan, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 2016. Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection. [Online]. bioRxiv. Available at: http://dx.doi.org/10.1101/068593

Han, Jun, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222 2016. Gender differences in CNV burden do not confound schizophrenia CNV associations. Scientific Reports 6 , 25986. 10.1038/srep25986

Isles, Anthony R. ORCID: https://orcid.org/0000-0002-7587-5712, Ingason, Andrés, Lowther, Chelsea, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Gawlick, Micha, Stöber, Gerald, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Little, Rosie B., Potter, Harry, Georgieva, Lyudmila, Pizzo, Lucilla, Ozaki, Norio, Aleksic, Branko, Kushima, Itaru, Ikeda, Masashi, Iwata, Nakao, Levinson, Douglas F., Gejman, Pablo V., Shi, Jianxin, Sanders, Alan R., Duan, Jubao, Willis, Joseph, Sisodiya, Sanjay, Costain, Gregory, Werge, Thomas M., Degenhardt, Franziska, Giegling, Ina, Rujescu, Dan, Hreidarsson, Stefan J., Saemundsen, Evald, Ahn, Joo Wook, Ogilvie, Caroline, Girirajan, Santhosh D., Stefansson, Hreinn, Stefansson, Kari, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Bassett, Anne and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2016. Parental origin of interstitial duplications at 15q11.2-q13.3 in schizophrenia and neurodevelopmental disorders. PLoS Genetics 12 (5) , e1005993. 10.1371/journal.pgen.1005993

Singh, Tarjinder, Swedish Schizophrenia Study, Kurki, Mitja I, Curtis, David, Purcell, Shaun M, Crooks, Lucy, McRae, Jeremy, Suvisaari, Jaana, Chheda, Himanshu, Blackwood, Douglas, Breen, Gerome, Pietiläinen, Olli, Gerety, Sebastian S., Ayub, Muhammad, Blyth, Moira, Cole, Trevor, Collier, David, Coomber, Eve L, Craddock, Nick ORCID: https://orcid.org/0000-0003-2171-0610, Daly, Mark J, Danesh, John, DiForti, Marta, Foster, Alison, Freimer, Nelson B., Geschwind, Daniel, Johnstone, Mandy, Joss, Shelagh, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Körkkö, Jarmo, Kuismin, Outi, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Hultman, Christina M., Iyegbe, Conrad, Lönnqvist, Jouko, Männikkö, Minna, McCarroll, Steve A., McGuffin, Peter, McIntosh, Andrew M., McQuillin, Andrew, Moilanen, Jukka S., Moore, Carmel, Murray, Robin M., Newbury-Ecob, Ruth, Ouwehand, Willem, Paunio, Tiina, Prigmore, Elena, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Roberts, David, Sambrook, Jennifer, Sklar, Pamela, Clair, David St, Veijola, Juha, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Williams, Hywel, Sullivan, Patrick F, Hurles, Matthew E., O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Palotie, Aarno, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Barrett, Jeffrey C., INTERVAL Study, DDD Study and UK10 K Consortium 2016. Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders. Nature Neuroscience 19 (4) , pp. 571-577. 10.1038/nn.4267

Fry, Andrew Evan ORCID: https://orcid.org/0000-0001-9778-6924, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Thompson, Rose, Mantripragada, Kiran ORCID: https://orcid.org/0000-0003-2070-8105, Blake, Penny, Jones, Glyn, Morgan, Sian, Jose, Sian, Mugalaasi, Hood, Archer, Hayley, McCann, Emma, Clarke, Angus John ORCID: https://orcid.org/0000-0002-1200-9286, Taylor, Clare, Davies, Sally, Gibbon, Frances, Te Water Naude, Johann, Hartley, Louise, Thomas, Gareth, White, Catharine, Natarajan, Jaya, Thomas, Rhys H., Drew, Cheney ORCID: https://orcid.org/0000-0002-4397-6252, Chung, Seo-Kyung, Rees, Mark I. ORCID: https://orcid.org/0000-0002-6168-9222, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Pilz, Daniela T. and Kerr, Michael Patrick 2016. Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy. BMC Medical Genetics 17 , -. 10.1186/s12881-016-0294-2

Singh, Tarjinder, Kurki, Mitja I., Curtis, David, Purcell, Shaun M., Crooks, Lucy, McRae, Jeremy, Suvisaari, Jaana, Chheda, Himanshu, Blackwood, Douglas, Breen, Gerome, Pietilainen, Olli, Gerety, Sebastian S., Ayub, Muhammad, Blyth, Moira, Cole, Trevor, Collier, David, Coomber, Eve L., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Daly, Mark J., Danesh, John, DiForti, Marta, Foster, Alison, Freimer, Nelson B., Geschwind, Daniel, Johnstone, Mandy, Joss, Shelagh, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Korkko, Jarmo, Kuismin, Outi, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Hultman, Christina M., Iyegbe, Conrad, Lonnqvist, Jouko, Mannikko, Minna, McCaroll, Steve A., McGuffin, Peter, McIntosh, Andrew M., McQuillin, Andrew, Moilanen, Jukka S., Moore, Carmel, Murray, Robin M., Newbury-Ecob, Ruth, Ouwehand, Willem, Paunio, Tiina, Prigmore, Elena, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Roberts, David, Sambrook, Jennifer, Sklar, Pamela, St Clair, David, Vejola, Juha, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Williams, Hywel, Swedish Schizophrenia Study, INTERVAL Study, DDD Study, UKK Consortium, Sullivan, Patrick F., Hurles, Matthew E., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Palotie, Aarno, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Barrett, Jeffrey C. 2016. Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders. Nature Neuroscience 19 , pp. 571-577. 10.1101/036384

Richards, Alexander, Leonenko, Ganna M ORCID: https://orcid.org/0000-0001-8025-661X, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Kavanagh, D, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Evans, Anna ORCID: https://orcid.org/0000-0002-2430-811X, Chambert, K. D., Moran, J. L., Goldstein, J., Neale, B. M., McCarroll, S. A., Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2016. Exome arrays capture polygenic rare variant contributions to schizophrenia. Human Molecular Genetics 25 (5) , pp. 1001-1007. 10.1093/hmg/ddv620

Tansey, Katherine E., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Linden, David Edmun Johannes ORCID: https://orcid.org/0000-0002-5638-9292, Ripke, S, Chambert, K D, Moran, J L, McCarroll, S A, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2015. Common alleles contribute to schizophrenia in CNV carriers [Erratum]. Molecular Psychiatry 21 , 1153. 10.1038/mp.2015.170

Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Isles, Anthony Roger ORCID: https://orcid.org/0000-0002-7587-5712, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2015. No evidence for enrichment in schizophrenia for common allelic associations at imprinted loci. PLoS ONE 10 (12) , -. 10.1371/journal.pone.0144172

Heyes, Samuel, Pratt, Wendy S., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Dahimene, Shehrazade, Ferron, Laurent, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Dolphin, Annette C. 2015. Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders. Progress in Neurobiology 134 , pp. 36-54. 10.1016/j.pneurobio.2015.09.002

Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Han, Jun, Kavanagh, David H., Chambert, Kimberly D., Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Moran, Jennifer L., McCarroll, Steven A., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2015. Novel findings from CNVs implicate inhibitory and excitatory signaling complexes in schizophrenia. Neuron 86 (5) , pp. 1203-1214. 10.1016/j.neuron.2015.04.022

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222 and Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053 2015. What a psychiatrist needs to know about copy number variants. BJPscyh Advances 21 (3) , pp. 157-163. 10.1192/apt.bp.113.012039

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2015. Genetics of schizophrenia. Current Opinion in Behavioral Sciences 2 , pp. 8-14. 10.1016/j.cobeha.2014.07.001

Green, E. K., Rees, E. ORCID: https://orcid.org/0000-0002-6168-9222, Walters, J. T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Smith, K-G, Forty, L., Grozeva, D. ORCID: https://orcid.org/0000-0003-3239-8415, Moran, J. L., Sklar, P., Ripke, S., Chambert, K. D., Genovese, G., McCarroll, S. A., Jones, I. ORCID: https://orcid.org/0000-0001-5821-5889, Jones, L. ORCID: https://orcid.org/0000-0001-5821-5889, Owen, M. J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, M. C. ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, N. ORCID: https://orcid.org/0000-0003-2171-0610 and Kirov, G. ORCID: https://orcid.org/0000-0002-3427-3950 2015. Copy number variation in bipolar disorder. Molecular Psychiatry 21 (1) , pp. 89-93. 10.1038/mp.2014.174

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Richards, Alexander, Howrigan, D., Kavanagh, D. H., Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Fromer, M., Ruderfer, D..M., Georgieva, Lyudmila, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Gormley, P., Palta, P., Williams, H., Dwyer, S., Johnson, J. S., Roussos, P., Barker, D. D., Banks, E., Milanova, V., Rose, S .A., Chambert, K., Mahajan, M, Scolnick, E. M., Moran, J. L., Tsuang, M. T., Glatt, S. J., Chen, W. J., Hwu, H.-G., Faraone, Stephen V., Roe, Cheri A., Chandler, Sharon D., Liu, Chih-Min, Liu, Chen-Chung, Yeh, Ling-Ling, Ouyang, Wen-Chen, Chan, Hung-Yu, Chen, Chun-Ying, Neale, B. M., Palotie, A., Sklar, P., Purcell, S. M., McCarroll, S .A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2015. Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia. Translational Psychiatry 5 (7) , e607. 10.1038/tp.2015.99

Georgieva, Lyudmila, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Moran, Jennifer L., Chambert, Kimberly D., Milanova, Vihra, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Purcell, Shaun, Sklar, Pamela, McCarroll, Steven, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2014. De novo CNVs in bipolar affective disorder and schizophrenia. Human Molecular Genetics 23 (24) , pp. 6677-6683. 10.1093/hmg/ddu379

Szatkiewicz, J. P., O'Dushlaine, C., Chen, G., Chambert, K., Moran, J. L., Neale, B. M., Fromer, M., Ruderfer, D., Akterin, S., Bergen, S. E., Kähler, A., Magnusson, P. K. E., Kim, Y., Crowley, J..J., Rees, E. ORCID: https://orcid.org/0000-0002-6168-9222, Kirov, G. ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, M. C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, M. J. ORCID: https://orcid.org/0000-0003-4798-0862, Walters, J. T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Scolnick, E., Sklar, P., Purcell, S., Hultman, C. M., McCarroll, S. A. and Sullivan, P. F. 2014. Copy number variation in schizophrenia in Sweden. Molecular Psychiatry 19 (7) , pp. 762-773. 10.1038/mp.2014.40

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2014. Authors' reply [Letter]. British Journal of Psychiatry 205 (1) , p. 78. 10.1192/bjp.205.1.78

Morris, D. W., Pearson, R. D., Cormican, P., Kenny, E. M., O'Dushlaine, C. T., Perreault, L.-P. L., Giannoulatou, E., Tropea, D., Maher, B. S., Wormley, B., Kelleher, E., Fahey, C., Molinos, I., Bellini, S., Pirinen, M., Strange, A., Freeman, C., Thiselton, D. L., Elves, R. L., Regan, R., Ennis, S., Dinan, T. G., McDonald, C., Murphy, K. C., O'Callaghan, E., Waddington, J. L., Walsh, D., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Grozeva, Detelina, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Stone, J., Scolnick, E., Purcell, S., Sklar, P., Coe, B., Eichler, E. E., Ophoff, R., Buizer, J., Szatkiewicz, J., Hultman, C., Sullivan, P., Gurling, H., Mcquillin, A., St Clair, D., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Blackwood, D., Johnstone, M., Donohoe, G., O'Neill, F. A., Kendler, K. S., Gill, M., Riley, B. P., Spencer, C. C. A. and Corvin, A. 2014. An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis. Human Molecular Genetics 23 (12) , pp. 3316-3326. 10.1093/hmg/ddu025

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Walters, James t. R. ORCID: https://orcid.org/0000-0002-6980-4053, Chambert, Kimberley D., O'Dushlaine, Colm, Szatkiewicz, Jin, Richards, Alexander L., Georgieva, Lyudmila, Mahoney-Davies, Gerwyn, Legge, Sophie E., Moran, Jennifer L., Genovese, Guilio, Levinson, Douglas, Morris, Derek W., Cormican, Paul, Kendler, Kenneth S., O'Neill, Francis A., Riley, Brian, Gill, Michael, Corvin, Aiden, Sklar, Pamela, Hultman, Christina H., Pato, Carlos, Pato, Michelle, Sullivan, Patrick F., Gejman, Pablo V., McCarroll, Stephen A., O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2014. CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. Human Molecular Genetics 23 (6) , pp. 1669-1676. 10.1093/hmg/ddt540

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Georgieva, Lyudmila, Isles, Anthony R. ORCID: https://orcid.org/0000-0002-7587-5712, Chambert, Kimberley D., Richards, Alexander L., Mahoney-Davies, Gerwyn, Legge, Sophie E., Moran, Jennifer L., McCarroll, Stephen A., O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2014. Analysis of copy number variations at 15 schizophrenia-associated loci. British Journal of Psychiatry 204 (2) , pp. 108-114. 10.1192/bjp.bp.113.131052

Fromer, Menachem, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Kavanagh, David, Williams, Hywel J. ORCID: https://orcid.org/0000-0001-7758-0312, Dwyer, Sarah, Gormley, Padhraig, Georgieva, Lyudmila, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Palta, Priit, Ruderfer, Douglas, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Humphreys, Isla, Johnson, Jessica S., Roussos, Panos, Barker, Douglas D., Banks, Eric, Milanova, Vihra, Grant, Seth G., Hannon, Eilis ORCID: https://orcid.org/0000-0001-6840-072X, Rose, Samuel A., Chambert, Kimberly, Mahajan, Milind, Scolnick, Edward M., Moran, Jennifer L., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Palotie, Aarno, McCarroll, Steven A., Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Sklar, Pamela, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Purcell, Shaun M. and O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 2014. De novo mutations in schizophrenia implicate synaptic networks. Nature 506 , pp. 179-184. 10.1038/nature12929

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Sanders, A., Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Chambert, K. D., Shi, J., Szatkiewicz, J., O'Dushlaine, C., Richards, Alexander L., Green, Elaine Karen, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Davies, Geraint, Legge, Sophie E., Moran, J. L., Pato, C., Pato, M., Genovese, G., Levinson, D., Duan, J., Moy, W., Göring, H. H. H., Morris, D., Cormican, P., Kendler, K. S., O'Neill, F. A., Riley, B., Gill, M., Corvin, A., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Sklar, P., Hultman, C., Sullivan, P. F., Gejman, P. V., McCarroll, S. A., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2013. Evidence that duplications of 22q11.2 protect against schizophrenia. Molecular Psychiatry n/a 10.1038/mp.2013.156

Guha, Saurav, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Darvasi, Ariel, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Ikeda, Masashi, Bergen, Sarah E., Magnusson, Patrik K., Cormican, Paul, Morris, Derek, Gill, Michael, Cichon, Sven, Rosenfeld, Jeffrey A., Lee, Annette, Gregersen, Peter K., Kane, John M., Malhotra, Anil K., Rietschel, Marcella, Nöthen, Markus M., Degenhardt, Franziska, Priebe, Lutz, Breuer, René, Strohmaier, Jana, Ruderfer, Douglas M., Moran, Jennifer L., Chambert, Kimberly D., Sanders, Alan R., Shi, Jianxin, Kendler, Kenneth, Riley, Brien, O’Neill,, Tony, Walsh, Dermot, Malhotra, Dheeraj, Corvin, Aiden, Purcell, Shaun, Sklar, Pamela, Iwata, Nakao, Hultman, Christina M., Sullivan, Patrick F., Sebat, Jonathan, McCarthy, Shane, Gejman, Pablo V., Levinson, Douglas F., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Lencz, Todd and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2013. Implication of a rare deletion at distal 16p11.2 in schizophrenia. JAMA Psychiatry 70 (3) , pp. 253-260. 10.1001/2013.jamapsychiatry.71

Chapman, J., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Harold, Denise, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Gerrish, Amy, Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Hollingworth, P, Stretton, A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2013. A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk. Human Molecular Genetics 22 (4) , pp. 816-824. 10.1093/hmg/dds476

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Georgieva, Lyudmila, Richards, Alexander, Chambert, Kimberly D., Davies, Gerwyn, Legge, Sophie E., Moran, Jennifer L., McCarroll, Steven A., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2013. The penetrance of copy number variations for schizophrenia and developmental delay. Biological Psychiatry 75 (5) , pp. 378-385. 10.1016/j.biopsych.2013.07.022

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2012. De Novo mutation in schizophrenia. Schizophrenia Bulletin 38 (3) , pp. 377-381. 10.1093/schbul/sbs047

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Ikeda, M., Ruderfer, D., Moran, J., Chambert, K., Toncheva, D., Georgieva, Lyudmila, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Fjodorova, Marija, Wollerton, Rebecca Louise, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Nikolov, Ivan, van de Lagemaat, L. N., Bayés, À., Fernandez, E., Olason, P. I., Böttcher, Y., Komiyama, N. H., Collins, M. O., Choudhary, J., Stefansson, K., Stefansson, H., Grant, S. G. N., Purcell, S., Sklar, P., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2012. De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia. Molecular Psychiatry 17 (2) , pp. 142-153. 10.1038/mp.2011.154

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2011. De novo rates and selection of schizophrenia-associated copy number variants. Biological Psychiatry 70 (12) , pp. 1109-1114. 10.1016/j.biopsych.2011.07.011